NP-MRD: Showing NP-Card for (10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene (NP0206436)

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Record Information

Version

2.0

Created at

2022-09-05 02:40:56 UTC

Updated at

2022-09-05 02:40:56 UTC

NP-MRD ID

NP0206436

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene

Description

(6AR)-4,5,6,6a,7,8-Hexahydro-1,2,10,11,12-pentamethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline belongs to the class of organic compounds known as homoaporphines. These are alkaloids derived from phenethylisoquinoline precursors by direct intramolecular oxidative coupling. They incorporate a nucleus A and are always pentaoxygenated at C- 1, -2, - 10, - 11, and - 12. The nitrogen function in ring B is usually N-methylated, but it may also be secondary. (10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene is found in Colchicum szovitsii. Based on a literature review very few articles have been published on (6aR)-4,5,6,6a,7,8-Hexahydro-1,2,10,11,12-pentamethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052204402D          

 29 32  0  0  1  0            999 V2000
    5.6487   -1.0952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3111   -0.3073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9613   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1730   -0.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9894    0.6557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7730    2.2232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4811    2.7712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2272    1.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0857    1.2489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2461    1.0136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4747    1.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2220    2.1395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5261    3.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8700    2.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6979    3.1455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1235    3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0816    2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8981    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5028    0.6557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3192   -0.1486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8336   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6586   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5309   -0.3918    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1923   -1.1838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0739    0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 25  1  0  0  0  0
 23 26  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 21 29  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    4.9150   -2.8108    1.6266 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5992   -1.6563    0.8876 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2991   -1.1819    0.7548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2697   -1.8866    1.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0091   -1.4210    1.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7807   -0.2568    0.5090 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7432    0.4487   -0.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    1.5509   -0.8704 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1925    1.4808   -2.2858 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0369   -0.0334    0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1289    0.5878   -0.5731 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5777    0.2573   -1.8750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5453    0.3955    0.3920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3989    1.7485    0.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8140    2.3099    0.7620 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1967    2.6001    2.1051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5279    2.5077    0.1832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3959    3.8882    0.2231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    4.7103   -0.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7386    1.9105   -0.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8747    0.5361   -0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7515   -0.2656    0.1179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0271   -1.7220    0.2409 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9029   -2.6040    0.4739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0987   -2.3064    1.7836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0168   -2.0964   -0.7351 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6145   -1.8791   -2.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2711   -1.4684   -0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1942    0.0030   -0.4916 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2393   -3.6601    1.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0395   -2.5917    2.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9267   -3.1449    1.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4751   -2.7869    1.9617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3425    2.1767   -2.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8801    0.4839   -2.5894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0451    1.8932   -2.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3564    1.0449   -2.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0274   -0.6537   -2.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6589   -0.0279   -1.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4827    2.2138    2.8378 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4151    3.6837    2.2219 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1641    2.0742    2.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7797    4.7704   -1.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3138    5.7562    0.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4076    4.3806    0.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6062    2.5356   -0.3062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6466   -1.7535    1.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060   -3.6856    0.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1865   -2.6004   -0.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7573   -1.7375    2.4327 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3491   -3.2126    2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5803   -1.4927   -2.1933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6119   -2.8862   -2.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3429   -1.2713   -2.6792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4631   -1.7331    0.6757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1138   -1.9233   -0.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5485    0.3959   -1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9986    0.4055    0.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 11 12  1  0
 10  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
  6 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 23 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 14 17  1  0
 29 21  1  0
 13 22  1  0
  4  5  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 23 47  1  1
 24 48  1  0
 24 49  1  0
 25 50  1  0
 25 51  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
M  END


  Mrv1652309052204402D          

 29 32  0  0  1  0            999 V2000
    5.6487   -1.0952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3111   -0.3073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661    0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9613   -0.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1730   -0.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9894    0.6557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7730    2.2232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4811    2.7712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2272    1.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0857    1.2489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2461    1.0136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4747    1.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2220    2.1395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5261    3.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8700    2.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6979    3.1455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1235    3.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0816    2.0211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8981    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5028    0.6557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3192   -0.1486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8336   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6586   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5309   -0.3918    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1923   -1.1838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0739    0.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1097    0.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  5 25  1  0  0  0  0
 23 26  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 21 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206436

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3[C@H](CCC4=C(C(OC)=C(OC)C(OC)=C4)C3=C1OC)N(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C23H29NO5/c1-24-10-9-14-12-16(25-2)21(27-4)20-18(14)15(24)8-7-13-11-17(26-3)22(28-5)23(29-6)19(13)20/h11-12,15H,7-10H2,1-6H3/t15-/m0/s1

> <INCHI_KEY>
VIZHHLWKNPFRJY-HNNXBMFYSA-N

> <FORMULA>
C23H29NO5

> <MOLECULAR_WEIGHT>
399.487

> <EXACT_MASS>
399.204573038

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
44.06826747142668

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(10S)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0^{2,7}.0^{14,18}]octadeca-1(17),2(7),3,5,14(18),15-hexaene

> <JCHEM_LOGP>
3.357624364333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
7.170340882022441

> <JCHEM_POLAR_SURFACE_AREA>
49.39000000000001

> <JCHEM_REFRACTIVITY>
112.9433

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(10S)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0^{2,7}.0^{14,18}]octadeca-1(17),2(7),3,5,14(18),15-hexaene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      10.544  -2.044   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.914  -0.574   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.523   0.316   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.395  -0.731   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.923  -0.277   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.580   1.224   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.709   2.271   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.043   4.150   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.365   5.173   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.181   1.817   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.757   2.426   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.360   2.331   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.193   1.892   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.620   3.179   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.014   3.994   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.582   5.656   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.491   4.227   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.169   5.872   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.097   7.062   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.019   3.773   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.676   2.271   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.805   1.224   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.463  -0.277   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.423  -1.481   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.963  -1.481   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       0.991  -0.731   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       0.359  -2.210   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.138   0.316   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.205   1.817   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    6   14   22                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   13   23                                                  
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24    5                                                       
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   21                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₉NO₅

Average Mass

399.4870 Da

Monoisotopic Mass

399.20457 Da

IUPAC Name

(10S)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0^{2,7}.0^{14,18}]octadeca-1(17),2(7),3,5,14(18),15-hexaene

Traditional Name

(10S)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0^{2,7}.0^{14,18}]octadeca-1(17),2(7),3,5,14(18),15-hexaene

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3[C@H](CCC4=C(C(OC)=C(OC)C(OC)=C4)C3=C1OC)N(C)CC2

InChI Identifier

InChI=1S/C23H29NO5/c1-24-10-9-14-12-16(25-2)21(27-4)20-18(14)15(24)8-7-13-11-17(26-3)22(28-5)23(29-6)19(13)20/h11-12,15H,7-10H2,1-6H3/t15-/m0/s1

InChI Key

VIZHHLWKNPFRJY-HNNXBMFYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Colchicum szovitsii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as homoaporphines. These are alkaloids derived from phenethylisoquinoline precursors by direct intramolecular oxidative coupling. They incorporate a nucleus A and are always pentaoxygenated at C- 1, -2, - 10, - 11, and - 12. The nitrogen function in ring B is usually N-methylated, but it may also be secondary.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Homoaporphines

Sub Class

Not Available

Direct Parent

Homoaporphines

Alternative Parents

Substituents

Homoaporphine
Tetrahydroisoquinoline
Anisole
Phenol ether
Alkyl aryl ether
Aralkylamine
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Ether
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen compound
Organooxygen compound
Amine
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.36	ChemAxon
pKa (Strongest Basic)	7.17	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	49.39 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.94 m³·mol⁻¹	ChemAxon
Polarizability	44.07 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9433090

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11258064

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene (NP0206436)

MOL for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

3D MOL for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

3D SDF for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

3D-SDF for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

PDB for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

3D PDB for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

SMILES for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

INCHI for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

Structure for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)

3D Structure for NP0206436 ((10s)-3,4,5,16,17-pentamethoxy-11-methyl-11-azatetracyclo[8.7.1.0²,⁷.0¹⁴,¹⁸]octadeca-1(17),2(7),3,5,14(18),15-hexaene)